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Technology in support of collaborative learning

technology education

Laferrière T.
GSID: 5UHqzF1o15QJ
P Resta, T Laferrière - Educational Psychology Review, 2007 - Springer

… Globally, the growth in the use of technology to support collaborative learning in higher education has attracted a rapidly growing number of research studies focused on some aspect of technology-supported collaborative learning examined from different theoretical …

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Resta, P., & Laferrière, T. (2007). Technology in support of collaborative learning. Educational Psychology Review, 19(1), 65-83.
Resta, Paul, and Thérèse Laferrière. "Technology in support of collaborative learning." Educational Psychology Review 19.1 (2007): 65-83.
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Digital equity and intercultural education

technology education

Laferrière T.
GSID: AY9zgCvdbp4J
P Resta, T Laferrière - Education and Information Technologies, 2015 - Springer

Digital equity and intercultural education continue to be areas of concern in the emerging knowledge-based society. The digital divide is present across the globe as the result of a …

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Resta, P., & Laferrière, T. (2015). Digital equity and intercultural education. Education and Information Technologies, 20(4), 743-756.
Resta, Paul, and Thérèse Laferrière. "Digital equity and intercultural education." Education and Information Technologies 20.4 (2015): 743-756.
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Temporal changes in bile acid levels and 12α-hydroxylation after Roux-en-Y gastric bypass surgery in type 2 diabetes.

International journal of obesity (2005)

Dutia R, Embrey M, O'Brien S, Haeusler RA, Agénor KK, Homel P, McGinty J, Vincent RP, Alaghband-Zadeh J, Staels B, le Roux CW, Yu J, Laferrère B.
PMID: 26952775
Int J Obes (Lond). 2016 Mar;40(3):554. doi: 10.1038/ijo.2015.250.

Since the publication of the above article it has been noted that the author S O'Brien should have been listed as CS O'Brien. The authors should therefore appear as follows: R Dutia, M Embrey, CS O'Brien, RA Haeusler, KK...

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Dutia R, Embrey M, O'Brien S, et al. Temporal changes in bile acid levels and 12α-hydroxylation after Roux-en-Y gastric bypass surgery in type 2 diabetes. Int J Obes (Lond). 2016;40(3):554doi: 10.1038/ijo.2015.250.
Dutia, R., Embrey, M., O'Brien, S., Haeusler, R. A., Agénor, K. K., Homel, P., McGinty, J., Vincent, R. P., Alaghband-Zadeh, J., Staels, B., le Roux, C. W., Yu, J., & Laferrère, B. (2016). Temporal changes in bile acid levels and 12α-hydroxylation after Roux-en-Y gastric bypass surgery in type 2 diabetes. International journal of obesity (2005), 40(3), 554. https://doi.org/10.1038/ijo.2015.250
Dutia, R, et al. "Temporal changes in bile acid levels and 12α-hydroxylation after Roux-en-Y gastric bypass surgery in type 2 diabetes." International journal of obesity (2005) vol. 40,3 (2016): 554. doi: https://doi.org/10.1038/ijo.2015.250
Dutia R, Embrey M, O'Brien S, Haeusler RA, Agénor KK, Homel P, McGinty J, Vincent RP, Alaghband-Zadeh J, Staels B, le Roux CW, Yu J, Laferrère B. Temporal changes in bile acid levels and 12α-hydroxylation after Roux-en-Y gastric bypass surgery in type 2 diabetes. Int J Obes (Lond). 2016 Mar;40(3):554. doi: 10.1038/ijo.2015.250. PMID: 26952775.
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Direct time-resolved detection of singlet oxygen in zeolite-based photocatalysts.

Langmuir : the ACS journal of surfaces and colloids

Cojocaru B, Laferrière M, Carbonell E, Parvulescu V, García H, Scaiano JC.
PMID: 18380514
Langmuir. 2008 May 06;24(9):4478-81. doi: 10.1021/la800441n. Epub 2008 Apr 02.

Singlet oxygen has been characterized spectroscopically as a product of the exposure of suspensions of zeolites containing oxidation catalysts. Spectroscopic and lifetime studies show that a part of the singlet oxygen formed reacts within the zeolite porous structure, while...

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Cojocaru B, Laferrière M, Carbonell E, et al. Direct time-resolved detection of singlet oxygen in zeolite-based photocatalysts. Langmuir. 2008;24(9):4478-81doi: 10.1021/la800441n.
Cojocaru, B., Laferrière, M., Carbonell, E., Parvulescu, V., García, H., & Scaiano, J. C. (2008). Direct time-resolved detection of singlet oxygen in zeolite-based photocatalysts. Langmuir : the ACS journal of surfaces and colloids, 24(9), 4478-81. https://doi.org/10.1021/la800441n
Cojocaru, Bogdan, et al. "Direct time-resolved detection of singlet oxygen in zeolite-based photocatalysts." Langmuir : the ACS journal of surfaces and colloids vol. 24,9 (2008): 4478-81. doi: https://doi.org/10.1021/la800441n
Cojocaru B, Laferrière M, Carbonell E, Parvulescu V, García H, Scaiano JC. Direct time-resolved detection of singlet oxygen in zeolite-based photocatalysts. Langmuir. 2008 May 06;24(9):4478-81. doi: 10.1021/la800441n. Epub 2008 Apr 02. PMID: 18380514.
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Weight-Independent Mechanisms of Glucose Control After Roux-en-Y Gastric Bypass.

Frontiers in endocrinology

Laferrère B, Pattou F.
PMID: 30250454
Front Endocrinol (Lausanne). 2018 Sep 10;9:530. doi: 10.3389/fendo.2018.00530. eCollection 2018.

Roux-en-Y gastric bypass results in large and sustained weight loss and resolution of type 2 diabetes in 60% of cases at 1-2 years. In addition to calorie restriction and weight loss, various gastro-intestinal mediated mechanisms, independent of weight loss,...

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Laferrère B, Pattou F. Weight-Independent Mechanisms of Glucose Control After Roux-en-Y Gastric Bypass. Front Endocrinol (Lausanne). 2018;9:530doi: 10.3389/fendo.2018.00530.
Laferrère, B., & Pattou, F. (2018). Weight-Independent Mechanisms of Glucose Control After Roux-en-Y Gastric Bypass. Frontiers in endocrinology, 9530. https://doi.org/10.3389/fendo.2018.00530
Laferrère, Blandine, and Pattou, François. "Weight-Independent Mechanisms of Glucose Control After Roux-en-Y Gastric Bypass." Frontiers in endocrinology vol. 9 (2018): 530. doi: https://doi.org/10.3389/fendo.2018.00530
Laferrère B, Pattou F. Weight-Independent Mechanisms of Glucose Control After Roux-en-Y Gastric Bypass. Front Endocrinol (Lausanne). 2018 Sep 10;9:530. doi: 10.3389/fendo.2018.00530. eCollection 2018. PMID: 30250454; PMCID: PMC6140402.
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Temporal Eating Patterns and Eating Windows among Adults with Overweight or Obesity.

Nutrients

Popp CJ, Curran M, Wang C, Prasad M, Fine K, Gee A, Nair N, Perdomo K, Chen S, Hu L, St-Jules DE, Manoogian ENC, Panda S, Sevick MA, Laferrère B.
PMID: 34960035
Nutrients. 2021 Dec 15;13(12). doi: 10.3390/nu13124485.

We aim to describe temporal eating patterns in a population of adults with overweight or obesity. In this cross-sectional analysis, data were combined from two separate pilot studies during which participants entered the timing of all eating occasions (>0...

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Popp CJ, Curran M, Wang C, et al. Temporal Eating Patterns and Eating Windows among Adults with Overweight or Obesity. Nutrients. 2021;13(12)doi: 10.3390/nu13124485.
Popp, C. J., Curran, M., Wang, C., Prasad, M., Fine, K., Gee, A., Nair, N., Perdomo, K., Chen, S., Hu, L., St-Jules, D. E., Manoogian, E. N. C., Panda, S., Sevick, M. A., & Laferrère, B. (2021). Temporal Eating Patterns and Eating Windows among Adults with Overweight or Obesity. Nutrients, 13(12), . https://doi.org/10.3390/nu13124485
Popp, Collin J, et al. "Temporal Eating Patterns and Eating Windows among Adults with Overweight or Obesity." Nutrients vol. 13,12 (2021). doi: https://doi.org/10.3390/nu13124485
Popp CJ, Curran M, Wang C, Prasad M, Fine K, Gee A, Nair N, Perdomo K, Chen S, Hu L, St-Jules DE, Manoogian ENC, Panda S, Sevick MA, Laferrère B. Temporal Eating Patterns and Eating Windows among Adults with Overweight or Obesity. Nutrients. 2021 Dec 15;13(12). doi: 10.3390/nu13124485. PMID: 34960035.
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SarkoSpin: A Technique for Biochemical Isolation and Characterization of Pathological TDP-43 Aggregates.

Bio-protocol

Pérez-Berlanga M, Laferrière F, Polymenidou M.
PMID: 33654921
Bio Protoc. 2019 Nov 20;9(22):e3424. doi: 10.21769/BioProtoc.3424. eCollection 2019 Nov 20.

TDP-43 is the main aggregating protein in neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD). Aggregated TDP-43 is resistant to diverse detergent solubilization, yet physiological TDP-43 and other abundant proteins commonly co-purify with pathological...

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Pérez-Berlanga M, Laferrière F, Polymenidou M. SarkoSpin: A Technique for Biochemical Isolation and Characterization of Pathological TDP-43 Aggregates. Bio Protoc. 2019;9(22):e3424doi: 10.21769/BioProtoc.3424.
Pérez-Berlanga, M., Laferrière, F., & Polymenidou, M. (2019). SarkoSpin: A Technique for Biochemical Isolation and Characterization of Pathological TDP-43 Aggregates. Bio-protocol, 9(22), e3424. https://doi.org/10.21769/BioProtoc.3424
Pérez-Berlanga, Manuela, et al. "SarkoSpin: A Technique for Biochemical Isolation and Characterization of Pathological TDP-43 Aggregates." Bio-protocol vol. 9,22 (2019): e3424. doi: https://doi.org/10.21769/BioProtoc.3424
Pérez-Berlanga M, Laferrière F, Polymenidou M. SarkoSpin: A Technique for Biochemical Isolation and Characterization of Pathological TDP-43 Aggregates. Bio Protoc. 2019 Nov 20;9(22):e3424. doi: 10.21769/BioProtoc.3424. eCollection 2019 Nov 20. PMID: 33654921; PMCID: PMC7853943.
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Drug-Nutraceutical Co-Crystal and Salts for Making New and Improved Bi-Functional Analgesics.

Pharmaceutics

Fulas OA, Laferrière A, Ayoub G, Gandrath D, Mottillo C, Titi HM, Stein RS, Friščić T, Coderre TJ.
PMID: 33255979
Pharmaceutics. 2020 Nov 26;12(12). doi: 10.3390/pharmaceutics12121144.

The discovery and development of effective analgesics is greatly lagging behind the steadily rising prevalence of chronic pain. Currently prescribed analgesics for chronic pain are lacking in efficacy mainly due to their narrowly-targeted mechanism of action. Driving neuronal hyperexcitability...

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Fulas OA, Laferrière A, Ayoub G, et al. Drug-Nutraceutical Co-Crystal and Salts for Making New and Improved Bi-Functional Analgesics. Pharmaceutics. 2020;12(12)doi: 10.3390/pharmaceutics12121144.
Fulas, O. A., Laferrière, A., Ayoub, G., Gandrath, D., Mottillo, C., Titi, H. M., Stein, R. S., Friščić, T., & Coderre, T. J. (2020). Drug-Nutraceutical Co-Crystal and Salts for Making New and Improved Bi-Functional Analgesics. Pharmaceutics, 12(12), . https://doi.org/10.3390/pharmaceutics12121144
Fulas, Oli Abate, et al. "Drug-Nutraceutical Co-Crystal and Salts for Making New and Improved Bi-Functional Analgesics." Pharmaceutics vol. 12,12 (2020). doi: https://doi.org/10.3390/pharmaceutics12121144
Fulas OA, Laferrière A, Ayoub G, Gandrath D, Mottillo C, Titi HM, Stein RS, Friščić T, Coderre TJ. Drug-Nutraceutical Co-Crystal and Salts for Making New and Improved Bi-Functional Analgesics. Pharmaceutics. 2020 Nov 26;12(12). doi: 10.3390/pharmaceutics12121144. PMID: 33255979; PMCID: PMC7761172.
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Effect on Nitrogen Balance, Thermogenesis, Body Composition, Satiety, and Circulating Branched Chain Amino Acid Levels up to One Year after Surgery: Protocol of a Randomized Controlled Trial on Dietary Protein During Surgical Weight Loss.

JMIR research protocols

Moizé V, Pi-Sunyer X, Vidal J, Miner P, Boirie Y, Laferrère B.
PMID: 27895003
JMIR Res Protoc. 2016 Nov 28;5(4):e220. doi: 10.2196/resprot.6438.

BACKGROUND: Bariatric surgery (BS), the most effective treatment for severe obesity, typically results in 40-50 kg weight loss in the year following the surgery. Beyond its action on protein metabolism, dietary protein intake (PI) affects satiety, thermogenesis, energy efficiency,...

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Moizé V, Pi-Sunyer X, Vidal J, et al. Effect on Nitrogen Balance, Thermogenesis, Body Composition, Satiety, and Circulating Branched Chain Amino Acid Levels up to One Year after Surgery: Protocol of a Randomized Controlled Trial on Dietary Protein During Surgical Weight Loss. JMIR Res Protoc. 2016;5(4):e220doi: 10.2196/resprot.6438.
Moizé, V., Pi-Sunyer, X., Vidal, J., Miner, P., Boirie, Y., & Laferrère, B. (2016). Effect on Nitrogen Balance, Thermogenesis, Body Composition, Satiety, and Circulating Branched Chain Amino Acid Levels up to One Year after Surgery: Protocol of a Randomized Controlled Trial on Dietary Protein During Surgical Weight Loss. JMIR research protocols, 5(4), e220. https://doi.org/10.2196/resprot.6438
Moizé, Violeta, et al. "Effect on Nitrogen Balance, Thermogenesis, Body Composition, Satiety, and Circulating Branched Chain Amino Acid Levels up to One Year after Surgery: Protocol of a Randomized Controlled Trial on Dietary Protein During Surgical Weight Loss." JMIR research protocols vol. 5,4 (2016): e220. doi: https://doi.org/10.2196/resprot.6438
Moizé V, Pi-Sunyer X, Vidal J, Miner P, Boirie Y, Laferrère B. Effect on Nitrogen Balance, Thermogenesis, Body Composition, Satiety, and Circulating Branched Chain Amino Acid Levels up to One Year after Surgery: Protocol of a Randomized Controlled Trial on Dietary Protein During Surgical Weight Loss. JMIR Res Protoc. 2016 Nov 28;5(4):e220. doi: 10.2196/resprot.6438. PMID: 27895003; PMCID: PMC5153533.
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Similar neuronal imprint and no cross-seeded fibrils in α-synuclein aggregates from MSA and Parkinson's disease.

NPJ Parkinson's disease

Laferrière F, Claverol S, Bezard E, De Giorgi F, Ichas F.
PMID: 35027576
NPJ Parkinsons Dis. 2022 Jan 13;8(1):10. doi: 10.1038/s41531-021-00264-w.

Aggregated alpha-synuclein (α-syn) is a principal constituent of Lewy bodies (LBs) and glial cytoplasmic inclusions (GCIs) observed respectively inside neurons in Parkinson's disease (PD) and oligodendrocytes in multiple system atrophy (MSA). Yet, the cellular origin, the pathophysiological role, and...

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Laferrière F, Claverol S, Bezard E, et al. Similar neuronal imprint and no cross-seeded fibrils in α-synuclein aggregates from MSA and Parkinson's disease. NPJ Parkinsons Dis. 2022;8(1):10doi: 10.1038/s41531-021-00264-w.
Laferrière, F., Claverol, S., Bezard, E., De Giorgi, F., & Ichas, F. (2022). Similar neuronal imprint and no cross-seeded fibrils in α-synuclein aggregates from MSA and Parkinson's disease. NPJ Parkinson's disease, 8(1), 10. https://doi.org/10.1038/s41531-021-00264-w
Laferrière, Florent, et al. "Similar neuronal imprint and no cross-seeded fibrils in α-synuclein aggregates from MSA and Parkinson's disease." NPJ Parkinson's disease vol. 8,1 (2022): 10. doi: https://doi.org/10.1038/s41531-021-00264-w
Laferrière F, Claverol S, Bezard E, De Giorgi F, Ichas F. Similar neuronal imprint and no cross-seeded fibrils in α-synuclein aggregates from MSA and Parkinson's disease. NPJ Parkinsons Dis. 2022 Jan 13;8(1):10. doi: 10.1038/s41531-021-00264-w. PMID: 35027576.
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Comparative study of the quenching of core and core-shell CdSe quantum dots by binding and non-binding nitroxides.

Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology

Heafey E, Laferrière M, Scaiano JC.
PMID: 17487312
Photochem Photobiol Sci. 2007 May;6(5):580-4. doi: 10.1039/b616616d. Epub 2007 Feb 13.

The quenching of core and core-shell CdSe quantum dots by TEMPO and 4-amino-TEMPO has been examined using steady state fluorescence spectroscopy. The efficiency of quenching is strongly dependent on the nanoparticle size, the binding properties of the nitroxide, and...

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Heafey E, Laferrière M, Scaiano JC. Comparative study of the quenching of core and core-shell CdSe quantum dots by binding and non-binding nitroxides. Photochem Photobiol Sci. 2007;6(5):580-4doi: 10.1039/b616616d.
Heafey, E., Laferrière, M., & Scaiano, J. C. (2007). Comparative study of the quenching of core and core-shell CdSe quantum dots by binding and non-binding nitroxides. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 6(5), 580-4. https://doi.org/10.1039/b616616d
Heafey, Eve, et al. "Comparative study of the quenching of core and core-shell CdSe quantum dots by binding and non-binding nitroxides." Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology vol. 6,5 (2007): 580-4. doi: https://doi.org/10.1039/b616616d
Heafey E, Laferrière M, Scaiano JC. Comparative study of the quenching of core and core-shell CdSe quantum dots by binding and non-binding nitroxides. Photochem Photobiol Sci. 2007 May;6(5):580-4. doi: 10.1039/b616616d. Epub 2007 Feb 13. PMID: 17487312.
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Ghrelin.

Molecular metabolism

Müller TD, Nogueiras R, Andermann ML, Andrews ZB, Anker SD, Argente J, Batterham RL, Benoit SC, Bowers CY, Broglio F, Casanueva FF, D'Alessio D, Depoortere I, Geliebter A, Ghigo E, Cole PA, Cowley M, Cummings DE, Dagher A, Diano S, Dickson SL, Diéguez C, Granata R, Grill HJ, Grove K, Habegger KM, Heppner K, Heiman ML, Holsen L, Holst B, Inui A, Jansson JO, Kirchner H, Korbonits M, Laferrère B, LeRoux CW, Lopez M, Morin S, Nakazato M, Nass R, Perez-Tilve D, Pfluger PT, Schwartz TW, Seeley RJ, Sleeman M, Sun Y, Sussel L, Tong J, Thorner MO, van der Lely AJ, van der Ploeg LH, Zigman JM, Kojima M, Kangawa K, Smith RG, Horvath T, Tschöp MH.
PMID: 26042199
Mol Metab. 2015 Mar 21;4(6):437-60. doi: 10.1016/j.molmet.2015.03.005. eCollection 2015 Jun.

BACKGROUND: The gastrointestinal peptide hormone ghrelin was discovered in 1999 as the endogenous ligand of the growth hormone secretagogue receptor. Increasing evidence supports more complicated and nuanced roles for the hormone, which go beyond the regulation of systemic energy...

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Müller TD, Nogueiras R, Andermann ML, et al. Ghrelin. Mol Metab. 2015;4(6):437-60doi: 10.1016/j.molmet.2015.03.005.
Müller, T. D., Nogueiras, R., Andermann, M. L., Andrews, Z. B., Anker, S. D., Argente, J., Batterham, R. L., Benoit, S. C., Bowers, C. Y., Broglio, F., Casanueva, F. F., D'Alessio, D., Depoortere, I., Geliebter, A., Ghigo, E., Cole, P. A., Cowley, M., Cummings, D. E., Dagher, A., Diano, S., Dickson, S. L., Diéguez, C., Granata, R., Grill, H. J., Grove, K., Habegger, K. M., Heppner, K., Heiman, M. L., Holsen, L., Holst, B., Inui, A., Jansson, J. O., Kirchner, H., Korbonits, M., Laferrère, B., LeRoux, C. W., Lopez, M., Morin, S., Nakazato, M., Nass, R., Perez-Tilve, D., Pfluger, P. T., Schwartz, T. W., Seeley, R. J., Sleeman, M., Sun, Y., Sussel, L., Tong, J., Thorner, M. O., van der Lely, A. J., van der Ploeg, L. H., Zigman, J. M., Kojima, M., Kangawa, K., Smith, R. G., Horvath, T., & Tschöp, M. H. (2015). Ghrelin. Molecular metabolism, 4(6), 437-60. https://doi.org/10.1016/j.molmet.2015.03.005
Müller, T D, et al. "Ghrelin." Molecular metabolism vol. 4,6 (2015): 437-60. doi: https://doi.org/10.1016/j.molmet.2015.03.005
Müller TD, Nogueiras R, Andermann ML, Andrews ZB, Anker SD, Argente J, Batterham RL, Benoit SC, Bowers CY, Broglio F, Casanueva FF, D'Alessio D, Depoortere I, Geliebter A, Ghigo E, Cole PA, Cowley M, Cummings DE, Dagher A, Diano S, Dickson SL, Diéguez C, Granata R, Grill HJ, Grove K, Habegger KM, Heppner K, Heiman ML, Holsen L, Holst B, Inui A, Jansson JO, Kirchner H, Korbonits M, Laferrère B, LeRoux CW, Lopez M, Morin S, Nakazato M, Nass R, Perez-Tilve D, Pfluger PT, Schwartz TW, Seeley RJ, Sleeman M, Sun Y, Sussel L, Tong J, Thorner MO, van der Lely AJ, van der Ploeg LH, Zigman JM, Kojima M, Kangawa K, Smith RG, Horvath T, Tschöp MH. Ghrelin. Mol Metab. 2015 Mar 21;4(6):437-60. doi: 10.1016/j.molmet.2015.03.005. eCollection 2015 Jun. PMID: 26042199; PMCID: PMC4443295.
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Showing 1 to 12 of 42 entries